If you are an experienced clinical research professional looking to advance your career in clinical operations, this Senior Clinical Research Associate (CRA) job in Bengaluru offers an excellent opportunity. Apotex is hiring skilled M.Pharm and B.Pharm graduates for a contract-based Senior Clinical Research Associate role at its Bioequivalence Center.
This opportunity is ideal for candidates with 3–6 years of experience in clinical operations, GCP, GLP compliance, and bioequivalence studies.
📌 Job Overview
- Position: Senior Clinical Research Associate (Contract Role)
- Company: Apotex
- Location: Bengaluru
- Experience Required: 3–6 Years
- Qualification: M.Pharm / B.Pharm
- Industry: Pharmaceutical & Life Sciences
- Employment Type: Full-Time (Temporary/Contractual)
- Salary: ₹3,00,000 – ₹6,00,000 per annum (as per experience)
🔬 Key Responsibilities – Senior Clinical Research Associate
The Senior Clinical Research Associate will be responsible for:
- Conducting clinical studies in compliance with GCP, GLP, SOPs, and regulatory guidelines
- Handling and execution of bioequivalence studies as per approved protocol
- Coordinating protocol training and study check-in activities
- Preparation and compilation of Trial Master File (TMF), Raw Data, CRFs, and Clinical Reports
- Ensuring accountability of study-specific forms and SOP documentation
- Performing dosing activities and supervising study procedures
- Reviewing collected data for completeness and protocol compliance
- Coordinating subject safety follow-ups and sample transfers
- Managing Nuleap form uploads and study check-out activities
- Archival and documentation management of completed studies
- Supporting regulatory documentation and compliance reporting
This clinical research associate job in Bengaluru requires strong operational execution skills and attention to regulatory compliance.
🎓 Eligibility Criteria
Educational Qualification:
- B.Pharm (Bachelor of Pharmacy)
- M.Pharm (Any Specialization)
Experience:
- Minimum 3 years and up to 6 years in Clinical Operations
- Hands-on experience in GCP/GLP compliance
- Experience in Bioequivalence (BE) studies preferred
Skills Required:
- Strong documentation and reporting skills
- Good communication skills
- Knowledge of regulatory guidelines
- Ability to work in cross-functional clinical teams
- Flexible to work as per study requirements
💼 Why Consider This Senior CRA Role?
- Exposure to regulated clinical research environment
- Experience in bioequivalence center operations
- Hands-on involvement in TMF, CRF, and clinical report preparation
- Strengthening regulatory compliance expertise
- Career progression in Clinical Research & Clinical Operations
This Senior Clinical Research Associate job at Apotex is suitable for professionals aiming to build expertise in bioequivalence studies and regulatory-compliant clinical research operations.
📥 How to Apply?
